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An evening of testimonial about “Living daily with lymphedema” hosted by Gisèle Laliberté, certified therapist – Virtual social gathering where people experiencing lymphedema share practical tips. Dressing, shoes, work, travel, exercise, self-management, budgeting – so many practical topics to help you in your daily life.
ZOOM presentation in French. Bilingual Q&A. This free event, organized by the LAQ, will take place on Thursday, June 13 at 7 p.m. Free and MANDATORY registration by clicking here.
We look forward to seeing you! This lymphedema event is made possible by the dedication of volunteer therapists and the Lymphedema Association of Quebec. The LAQ’s mission is to support people at risk and those affected by lymphedema, while raising awareness of lymphedema as a chronic disease among health professionals. |
The Lymphedema Association of Québec provides support, education, and awareness to people living with lymphedema, as well as their families, friends, and healthcare professionals. We provide information and educate about lymphedema and its causes, risk reduction, and treatments for this chronic disease, and encourage scientific research leading to a cure.
Lymphedema Association of Québec
Therapeutic Support Program
1 866 979-2463
514 979-2463
Mailing address
CP 152, Bureau Chef Branch,
Saint-Hyacinthe,
QC, J2S 7B4
Telephone
1 866 979-2463 / 514 979-2463
Email
aql@infolympho.ca
Website
www.infolympho.ca
© 2023 Lymphedema Association of Québec. All rights reserved. | Credits